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肺炎链球菌对大环内酯类和酮内酯类药物的耐药性

Macrolide and ketolide resistance with Streptococcus pneumoniae.

作者信息

Doern Gary V

机构信息

Clinical Microbiology Laboratories, University of Iowa Hospital and Clinics, 200 Hawkins Drive, Iowa City, IA 52242, USA.

出版信息

Med Clin North Am. 2006 Nov;90(6):1109-24. doi: 10.1016/j.mcna.2006.07.010.

Abstract

Antimicrobial agents in the macrolide family have long been considered drugs of potential utility in the management of infections caused by Streptococcus pneumoniae. However, with the emergence of macrolide resistance, the clinical value of macrolides in pneumococcal infections is threatened. In part, as a consequence of the development of macrolide resistance, recently the first agent in the ketolide antimicrobial class, telithromycin, was developed and introduced into clinical practice. The ketolides are macrolide antimicrobials whose chemistry has been modified so as avoid the effects of the most common mechanisms of macrolide resistance with S pneumoniae. This discussion reviews the current state of resistance to macrolides and ketolides with S pneumoniae in North America.

摘要

大环内酯类抗菌药物长期以来一直被认为是治疗肺炎链球菌感染的潜在有效药物。然而,随着大环内酯类耐药性的出现,大环内酯类药物在肺炎球菌感染中的临床价值受到了威胁。部分由于大环内酯类耐药性的发展,最近酮内酯类抗菌药物中的首个药物泰利霉素被研发并引入临床实践。酮内酯类是大环内酯类抗菌药物,其化学结构已被修饰,以避免肺炎链球菌对大环内酯类产生耐药性的最常见机制的影响。本讨论回顾了北美地区肺炎链球菌对大环内酯类和酮内酯类耐药性的现状。

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